GUDIDData
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eudamed_udi Primary ID: 05055455503373

Medial Rotation Knee (UDI 05055455503373)

Manufactured by MatOrtho Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medial Rotation Knee - Primary ID 05055455503373

Device Regulatory Overview

The Medial Rotation Knee (Model/Catalog Number: 156-010) is a medical device manufactured by MatOrtho Limited. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
156-010
Product Code / EMDN
P0909030101
Device Name
Medial Rotation Knee Femur
Database Sync Date
2026-08-09 16:30:42

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Medial Rotation Knee?

The registered manufacturer of record for Medial Rotation Knee is MatOrtho Limited.

What is the Primary UDI-DI identifier for Medial Rotation Knee?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055455503373.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by MatOrtho Limited

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